Transporters, Ion channel, putative
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HVZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 13 |
GO:0005216 | monoatomic ion channel activity | 4 | 13 |
GO:0005227 | calcium activated cation channel activity | 6 | 13 |
GO:0005261 | monoatomic cation channel activity | 5 | 13 |
GO:0005267 | potassium channel activity | 6 | 13 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 13 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 13 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 13 |
GO:0015267 | channel activity | 4 | 13 |
GO:0015269 | calcium-activated potassium channel activity | 7 | 13 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 13 |
GO:0016286 | small conductance calcium-activated potassium channel activity | 8 | 13 |
GO:0022803 | passive transmembrane transporter activity | 3 | 13 |
GO:0022836 | gated channel activity | 5 | 13 |
GO:0022839 | monoatomic ion gated channel activity | 6 | 13 |
GO:0022857 | transmembrane transporter activity | 2 | 13 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 13 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 13 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.339 |
CLV_MEL_PAP_1 | 3 | 9 | PF00089 | 0.409 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.570 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.642 |
DEG_SCF_FBW7_1 | 369 | 376 | PF00400 | 0.759 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.782 |
DEG_SPOP_SBC_1 | 435 | 439 | PF00917 | 0.758 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.638 |
DOC_PP4_MxPP_1 | 128 | 131 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.716 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 247 | 254 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 494 | 502 | PF00244 | 0.739 |
LIG_Actin_WH2_2 | 356 | 372 | PF00022 | 0.728 |
LIG_APCC_ABBA_1 | 401 | 406 | PF00400 | 0.720 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.643 |
LIG_CaM_IQ_9 | 299 | 314 | PF13499 | 0.561 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.643 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.622 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.323 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.598 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.637 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.625 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.585 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.602 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.645 |
LIG_GBD_Chelix_1 | 202 | 210 | PF00786 | 0.439 |
LIG_GBD_Chelix_1 | 70 | 78 | PF00786 | 0.423 |
LIG_LIR_Gen_1 | 136 | 147 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 151 | 158 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 320 | 328 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.729 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.726 |
LIG_MYND_3 | 442 | 446 | PF01753 | 0.783 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.339 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.645 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.469 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.370 |
LIG_SH2_SRC | 152 | 155 | PF00017 | 0.398 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.651 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.743 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.767 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.611 |
LIG_SUMO_SIM_anti_2 | 478 | 485 | PF11976 | 0.666 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.634 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.355 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.304 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.472 |
MOD_CDK_SPK_2 | 373 | 378 | PF00069 | 0.743 |
MOD_CDK_SPK_2 | 388 | 393 | PF00069 | 0.720 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.600 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.552 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.624 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.607 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.529 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.700 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.716 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.713 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.755 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.660 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.295 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.612 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.726 |
MOD_Cter_Amidation | 396 | 399 | PF01082 | 0.554 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.587 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.562 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.522 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.671 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.435 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.526 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.681 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.610 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.551 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.679 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.719 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.626 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.607 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.720 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.744 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.701 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.691 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.608 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.481 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.556 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.313 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.219 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.586 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.548 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.589 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.770 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.783 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.614 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.639 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.313 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.340 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.655 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.600 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.693 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.519 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.616 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.585 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.350 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.639 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.686 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.766 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.362 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.567 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.626 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.304 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.384 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.381 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.573 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.488 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.558 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.327 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.399 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.562 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.668 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.341 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.460 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.655 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.725 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.721 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.657 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.704 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 400 | 409 | PF00179 | 0.763 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.723 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.307 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W7 | Leptomonas seymouri | 62% | 98% |
A0A0S4IWT9 | Bodo saltans | 30% | 95% |
A0A0S4IZM8 | Bodo saltans | 36% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 28% | 94% |
A0A1X0NP80 | Trypanosomatidae | 38% | 100% |
A0A3Q8I9U0 | Leishmania donovani | 100% | 100% |
A0A422NNJ1 | Trypanosoma rangeli | 40% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 31% | 98% |
A4H7L1 | Leishmania braziliensis | 76% | 100% |
E9APP7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QFT2 | Leishmania major | 96% | 100% |